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Senior Medical Writer Ii

6+ years
Not Disclosed
10 April 18, 2025
Job Description
Job Type: Hybrid Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Medical Writer II

Location: India
Job Category: Medical Writing / Clinical Research

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About ProPharma:

ProPharma has spent the past 20 years improving patient health and wellness by empowering biotech, pharmaceutical, and medical device organizations with expert guidance. Through an advise-build-operate model, ProPharma partners with clients across the entire product lifecycle, offering regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology services. ProPharma delivers customizable solutions to de-risk and accelerate its partners' drug and device programs.

Position Overview:

ProPharma is seeking a Senior Medical Writer II who will author, edit, and manage the development of a variety of high-quality clinical, safety, regulatory, and disclosure documents across all phases of clinical research. This role also includes leadership responsibilities, such as supervising and mentoring less experienced writers.

Essential Functions:

  • Independently author and edit clinical, regulatory, safety, and device documents including protocols, study reports, IBs, ICFs, DSURs, plain language summaries, and complex documents (e.g., PBRERs, NDAs, BLAs, MAAs, eCTD submissions).

  • Supervise, train, and mentor junior medical writers as needed.

  • Ensure compliance with ICH E3/E6(R2), EU MDR/IVDR, internal SOPs, client standards, and approved templates.

  • Manage client communications, expectations, and project deliverable timelines with minimal supervision.

  • Lead internal and client meetings, including project kickoffs and comment review sessions.

  • Collaborate with subject matter experts across clinical operations, data management, biostatistics, and regulatory affairs to produce deliverables.

  • Coordinate quality control (QC) reviews of documents and maintain detailed audit trails.

  • Review statistical analysis plans and related outputs for content, grammar, formatting, and consistency.

  • Perform peer and QC reviews of documents authored by other writers when necessary.

  • Assist in administrative project tasks, such as maintaining timelines and updating trackers.

  • Stay current with industry practices and regulatory requirements.

  • Work within assigned budgets and notify management of any out-of-scope work.

  • Manage multiple projects simultaneously and proactively seek assistance when needed.

  • Participate in departmental initiatives and process improvements.

  • Other duties as assigned.

Necessary Skills and Abilities:

  • Advanced knowledge of clinical research principles and the ability to present complex clinical data.

  • Strong understanding of FDA regulations, global regulatory standards, and submission requirements.

  • Proficiency in MS Word, including skills in creating tables, graphs, and figures.

  • Excellent project management, communication, and attention to detail skills.

  • Fluency in English and familiarity with American Medical Association (AMA) writing style.

  • Strong relationship-building and strategic collaboration abilities.

  • Proactive, solutions-oriented thinker with strong time-management skills.

  • Ability to work independently and effectively within a collaborative environment.

  • Demonstrates a growth mindset and positive attitude toward work.

Educational Requirements:

  • Bachelor's degree or higher, preferably in a medical or scientific discipline.

Experience Requirements:

  • Minimum of 6 years of experience writing clinical and/or regulatory documents for drugs, biologics, and/or medical devices/diagnostics within a CRO, pharmaceutical, or biotechnology environment.

  • Other educational or professional experience may also be considered on a case-by-case basis.

Workplace Commitment:

ProPharma fosters a diverse, equitable, and inclusive environment where employees are encouraged to bring their authentic selves to work. As an Equal Opportunity Employer, ProPharma creates a supportive workplace where innovation and collaboration thrive.

Additional Information:

  • Unsolicited resumes from third-party recruiters will not be accepted.

  • No phone calls or emails regarding this posting, please.